Identifying the need for a multidisciplinary approach for early recognition of mucopolysaccharidosis VI (MPS VI). (Q48220787)

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6 March 2020

title

Identifying the need for a multidisciplinary approach for early recognition of mucopolysaccharidosis VI (MPS VI) (English)

1 reference

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6 March 2020

main subject

mucopolysaccharidosis VI

1 reference

19

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6 March 2020

author name string

Yew Sing Choy

1

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6 March 2020

Kaustuv Bhattacharya

2

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6 March 2020

Shanti Balasubramaniam

3

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6 March 2020

Michael Fietz

4

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6 March 2020

Antony Fu

5

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6 March 2020

Anita Inwood

6

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6 March 2020

Dong-Kyu Jin

7

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6 March 2020

Ok-Hwa Kim

8

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6 March 2020

Motomichi Kosuga

9

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6 March 2020

Young Hee Kwun

10

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6 March 2020

Hsiang-Yu Lin

11

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6 March 2020

Shuan-Pei Lin

12

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6 March 2020

Nancy J Mendelsohn

13

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6 March 2020

Torayuki Okuyama

14

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6 March 2020

Hasri Samion

15

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6 March 2020

Adeline Tan

16

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6 March 2020

Akemi Tanaka

17

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6 March 2020

Verasak Thamkunanon

18

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6 March 2020

Teck-Hock Toh

20

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6 March 2020

Albert D Yang

21

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6 March 2020

Jim McGill

22

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6 March 2020

publication date

26 March 2015

1 reference

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Molecular Genetics and Metabolism

6 March 2020

published in

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6 March 2020

volume

115

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6 March 2020

page(s)

41-47

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6 March 2020

issue

1

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Endocardial fibroelastosis in mucopolysaccharidosis type VI.

6 March 2020

cites work

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2015.03.005

Acute infantile cardiomyopathy as a presenting feature of mucopolysaccharidosis VI

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2015.03.005

Threshold effect of urinary glycosaminoglycans and the walk test as indicators of disease progression in a survey of subjects with Mucopolysaccharidosis VI (Maroteaux-Lamy syndrome)

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2015.03.005

Enzyme replacement therapy for mucopolysaccharidosis VI from 8 weeks of age--a sibling control study

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2015.03.005

Enzyme replacement therapy attenuates disease progression in two Japanese siblings with mucopolysaccharidosis type VI.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2015.03.005

Mucopolysaccharidosis VI.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2015.03.005

Spondyloepiphyseal dysplasias and bilateral legg-calvé-perthes disease: diagnostic considerations for mucopolysaccharidoses

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2015.03.005

Expert recommendations for the laboratory diagnosis of MPS VI.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2015.03.005

Mucopolysaccharidosis IVA (Morquio A syndrome) and VI (Maroteaux-Lamy syndrome): under-recognized and challenging to diagnose.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2015.03.005

Clinical characteristics of adults with slowly progressing mucopolysaccharidosis VI: a case series.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2015.03.005

Difficulties in diagnosing slowly progressive mucopolysaccharidosis VI: A case series

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2015.03.005

Cardiovascular manifestations of mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome).

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2015.03.005

Cardiac disease in patients with mucopolysaccharidosis: presentation, diagnosis and management

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2015.03.005

Mucopolysaccharidosis type VI: a predominantly cardiac phenotype associated with homozygosity for p.R152W mutation in the ARSB gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2015.03.005

10.1016/J.YMGME.2015.03.005

7 January 2021

Identifiers

DOI

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6 March 2020

1 reference